Cyphostemmin A
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IUPAC name 8-(3,5-dihydroxyphenyl)-6,7-bis(4-hydroxyphenyl)-5,8-dihydronaphthalene-1,3-diol | |
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3D model (JSmol) |
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CompTox Dashboard (EPA) |
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InChI
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Properties | |
Chemical formula | C28H22O6 |
Molar mass | 454.478 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references |
Chemical compound
Cyphostemmin A is an oligostilbene found in Cyphostemma crotalarioides (Vitaceae).[1]
See also
- Cyphostemmin B
References
- ^ Ducrot, Paul-Henri; Kollmann, Albert; Bala, Adil E.; Majira, Amel; Kerhoas, Lucien; Delorme, Robert; Einhorn, Jacques (1998). "Cyphostemmins A-B, two new antifungal oligostilbenes from Cyphostemma crotalarioides (Vitaceae)". Tetrahedron Letters. 39 (52): 9655–9658. doi:10.1016/S0040-4039(98)02207-2.
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Oligostilbenoids and their glycosides
- Diptoindonesin C
- Diptoindonesin F
- Gnetin H
- Hemsleyanol D
- Isohopeaphenol
- Laetevirenol A, B, C, D and E
- Suffruticosol A and B
- Viniferal
- E-ω-viniferin
- Z-ω-viniferin
- Diptoindonesin G
- Jezonodione
- B
- Scirpusin A
- Tibeticanol (piceatannol dimer)
- Amurensin B
- Gnetin E
- Gneyulin A
- Johorenol A
- Ampelopsin E
- Vaticanol G
- Dibalanocarpol
- Gnetin J (3"-hydroxygnetin E)
- Gnetin K (3"-methoxygnetin E)
- Gnetuhainin R (isorhapontigenin tetramer)
- Laetevirenol F and G
(five units or more)
- Vaticanol D, H, I and J
of resveratrol
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Tetramers |
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Pentamers |
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Higher polymers |
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- Diptoindonesin A (C-glucoside of ε-viniferin)
- Foeniculoside I (glucoside of miyabenol C), II, III and IV
- Laevifonol (an ε-viniferin-ascorbic acid hybrid compound)
- Laevifoside (O-glucoside of ampelopsin A)
This article about an aromatic compound is a stub. You can help Wikipedia by expanding it. |
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